Clinical Research Data Specialist

umiami; Miami (FL); Hybrid; USD 50.000 - 70.000; Vollzeit

Zusammenfassung

The University of Miami/UHealth department of SCCC is seeking a Hybrid Full Time Clinical Research Data Specialist to work in Miami, FL. The role involves extracting clinical data from EMRs and other sources, entering it into data capture systems, and maintaining study documentation in line with SOPs under PI oversight.

Responsibilities include coordinating with monitors, resolving data clarifications, preparing source data worksheets, and ensuring regulatory compliance across assigned studies.

Qualifikationen

• Ability to learn new procedures, technologies, and protocols.
• Team collaboration with multidisciplinary staff.
• Proficiency with office software and data systems.

Aufgaben

• Extract clinical data from EMR or other sources and enter it into data capture systems.
• Maintain study logs and prepare source data worksheets for each study.
• Address data clarifications and coordinate with monitors and PI as needed.
• Ensure regulatory compliance and adherence to SOPs and protocols.

Kenntnisse

Learning agility

Teamwork

Technical proficiency

Communication

Ausbildung

High school diploma or equivalent

Jobbeschreibung

Current Employees:

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Clinical Research Data Specialist

The University of Miami/UHealth department of SCCC has an exciting opportunity for a Hybrid Full Time Clinical Research Data Specialist to work in Miami, FL. The Clinical Research Data Specialist assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures, under the supervision of the Principal Investigator (PI) and supervisor. The Clinical Research Data Specialist is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to SOPs, and all applicable regulations and guidelines.

• Extracts clinical data and research data from electronic medical records and other sources and enters this data in the clinical paper-based or electronic data capture system for each assigned study.
• Manages a workload of studies commensurate to level of experience
• Answers data clarifications (i.e., data queries) for each study.
• Schedules and meets with study monitors and assures patient cases are ready for each monitor visit and items are addressed after each monitoring visit.
• Develops source data worksheets specific to each assigned study.
• Assures clinical issues from monitoring reports are addressed and closed out before the next monitoring visit.
• Assures all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.
• Maintains logs (i.e., TAS submissions, Velos etc.) in a timely manner according to department SOPs.
• Participates in site initiation visits (SIV), monitoring visits and participates in site disease group (SDG) team and PI oversight meetings as required.
• Assists multidisciplinary team in research activities.
• Maintains study binders and filings according to protocol requirements and department policy.
• Adheres to all UM and department policies and procedures.
• Compiles patient data for Investigator review to determine patient eligibility for protocol enrollment.
• Maintains screening, enrollment, adverse event, deviation, tumor measurement, concomitant medication, delegation and other sponsor and/or protocol specific logs.
• Ensures work environment is organized and functions efficiently. Participates in a collaborative, empowered work environment as demonstrated through teamwork.
• Demonstrates a level of professional practice that supports the delivery of appropriate care and positive working relationships throughout the medical center.
• Adheres to University and unit-level policies and procedures and safeguards University assets.

This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.

Core Qualifications

• High School Diploma or equivalent/relevant experience
• No previous experience required

Knowledge, Skills and Abilities:

• Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
• Teamwork: Ability to work collaboratively with others and contribute to a team environment.
• Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
• Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.

Any relevant education, certifications and/or work experience may be considered.

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.

The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.

Job Status: Full time

Employee Type: Staff